# FDA recall D-0870-2021

> **Washington Homeopathic Products, Inc.** · Class II · drug recall initiated 2021-08-20.

## Product

La Core LCL-2-0191 Blend, 149,980ml 20% Alcohol, WHP Homeopathic Medicine, For Manufacturing Only, Liter LCL-2-0191-Bend: 12% Lycopodium Clavatum 10X, 12% Carbo Vegetabilis 16X, 12% Natrum Muriaticum 9X, 12% Calcarea Carbonica 12X, 10% Hypothalamus 30X, 6% Pituitarum Posterium 12X,  6% Pituitarum Posterium 30C, 3% Natrum Phosphoricum 12X, 3% Graphites 30X, 3# Agnus Castus 6X, 3% Thiosinaminum 8X, 3% Phytolacca Decandra 12X, 3% Magnesia Phosphorica 10X, 3% Ornithogalum Umbellatum 6X, 3% Chelidonium Majus 6X, 3% Quercus Robur 14X, 3% Nux Vomica 30X,  Manufactured by Washington Homeopathic Products 260 JR Hawvermale Way, Berkeley Springs, WV, 25411.

## Reason for recall

Out-of-specification test results obtained for identification testing based on HPTLC analysis.

## Distribution

Distributed Nationwide in the USA

## Key facts

- **Recall number:** D-0870-2021
- **Recalling firm:** Washington Homeopathic Products, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-08-20
- **Report date:** 2021-10-06
- **Termination date:** 2022-06-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Berkeley Springs, WV, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0870-2021

## Citation

> AI Analytics. FDA recall D-0870-2021. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/D-0870-2021. Source: US FDA. Licensed CC0.

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